1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid

Base Information

Chemical Name:1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid
CAS No.:1414362-01-8
Molecular Formula:C₂₁H₁₈F₃N₃O₄
Molecular Weight:433.387
Hs Code.:

Synonyms:1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid

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Chemical Property of 1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid

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Technology Process of 1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid

There total 4 articles about 1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 50.0%

: 1414361-92-4
ethyl 1-(4-((3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl))-1H-pyrrole-2-carboxylate

: 1414362-01-8
1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid

Guidance literature:: With water; potassium hydroxide; In tetrahydrofuran; methanol; at 90 ℃; for 0.25h; Microwave irradiation;
DOI:10.1021/jm301194c

Reference yield:

: 1138159-55-3
ethyl 1-(4-(aminomethyl)benzyl)-1H-pyrrole-2-carboxylate

: 1414362-01-8
1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C / Inert atmosphere

2: potassium hydroxide; water / methanol; tetrahydrofuran / 0.25 h / 90 °C / Microwave irradiation

With water; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm301194c

Reference yield:

: 17201-43-3
4-cyanobenzyl bromide

: 1414362-01-8
1-(4-(3-((4-(trifluoromethoxy)phenyl)ureido)methyl)benzyl)-1H-pyrrole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: tetra-(n-butyl)ammonium iodide; sodium hydroxide / dichloromethane / 0 - 20 °C

2: hydrogen / methanol / 20 °C / 4500.45 Torr

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C / Inert atmosphere

4: potassium hydroxide; water / methanol; tetrahydrofuran / 0.25 h / 90 °C / Microwave irradiation

With water; hydrogen; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm301194c